Nickie Coby (puppybraille) wrote,
Nickie Coby
puppybraille

An annoying, but refreshing question

Today, I went to the pain clinic. Rather than talk about how I don't like that I'm still dealing with RSD, and that it's still chronic pain, and that I don't like it at all, I'll tell you about another part of the visit.

The nurse practitioner I work with is very kind (everyone there is). Today, as with the previous few visits, she asked if I could still identify all of my medications. I must have looked annoyed (which I'm somewhat repentant about), because she said she was sorry, but she would continue to ask this question.

Yes, I'm annoyed. But in many ways, I am so glad to see this question being asked. If you disagree, you might take a look at these two articles provided by the
American Foundation for the Blind

The reality is that while I have plenty of tools at my disposal such as Braille labels, rubber bands, a good sense of touch and years of blindness experience, not everyone does. And medications are potent. There is always a risk when someone takes a drug. But that risk gets much worse if the medication isn't taken properly. And the question still stands: how do you take your meds properly if you can't identify them?

While I do feel some annoyance at answering the question, I feel grattitude that the doctors, nurse practitioners and nurses at my clinic care enough to ask the question. I can imagine all too clearly a situation like the following made up case study:

Mrs. Johnson, a 75-year-old woman has been healthy for most of her life. She hasn't needed many medications. She's begun to lose her sight, and the problem has been great enough that her glasses no longer correct her vision enough, and she is considered legally blind.

Mrs. Johnson begins having severe pain, we'll say due to shingles nerve damage. She begins taking a few medications, which have different dosing instructions, but feel similar.

Not wanting to bother anyone, Mrs. Johnson doesn't tell anyone that she sometimes has trouble identifying her medicines.

One day, Mrs. Johnson takes too much of one medication. Unfortunately, it's one which can easily be over-dosed. In addition, because Mrs. Johnson doesn't know which medications she's taking, she takes none of a medication which should not be stopped abruptly. This causes severe symptoms, and a hospitalization.

I obviously don't have enough medical background to give specifics. What I do know is that this is still plausable. I would much rather answer a simple question than have the issue overlooked.

One additional concern I do have is what if the people who most need to be asked this question are the ones no one thinks to ask? Is Mrs. Johnson going to mention her failing vision to the doctor? It's a sobering reminder that the people who could most need my interventions as a social worker might be the ones I wouldn't expect to need it. And the questions I might need to ask most might seem like the ones I need to ask least.

I'll certainly be more patient with questions like this. I'd be interested in knowing if you've ever been asked this question, and even if you haven't, how would you react to it? Please feel free to leave a comment!

Tags: chronic pain, disability related, health, rsd sucks, social work
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